Evidence map›Paper›PMID 17549610›Full record

ReviewJournal of mammary gland biology and neoplasia2007

MTA family of transcriptional metaregulators in mammary gland morphogenesis and breast cancer.

Rajesh R Singh, Rakesh Kumar

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of mammary gland biology and neoplasia, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.7field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Prognostic correlation between MTA2 expression level and colorectal cancer.International journal of clinical and experimental pathology · 2015
    Article
  9. Article
  10. Review
  11. Role of MTA2 in human cancer.Cancer metastasis reviews · 2014
    Review
  12. Article
  13. MTA1 promotes nasopharyngeal carcinoma growth in vitro and in vivo.Journal of experimental & clinical cancer research : CR · 2013
    Article
  14. MTA-1 expression is associated with metastasis and epithelial to mesenchymal transition in colorectal cancer cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Rajesh R SinghMolecular and Cellular Oncology, The University of Texas, M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Rakesh Kumar
The University of Texas MD Anderson Cancer Center · US

Funding

Role of Metastatic Tumor Antigen-1 in Mammary GlandR01CA098823 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KUMAR, RAKESH · 2003 to 2013
$3.1M
RECEPTOR BLOCKADE FOR BREAST CANCERR01CA065746 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KUMAR, RAKESH · 1999 to 2007
$1.9M
LABORATORY STUDY OF CHEMOTHERAPY PLUS RECEPTOR BLOCKADEU01CA065746 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI KUMAR, RAKESH · 1995 to 1998
–
NCI NIH HHS CA65746NCI NIH HHS CA98823
6 · The paper itself

Abstract

Since breast cancer and its associated metastasis are a global health problem and a major cause of mortality among women, research efforts to understand the development, morphogenesis, and functioning of the mammary gland are a high priority. Myriad signaling pathways, transcription factors, and associated transcriptional coregulators have been identified in both normal functioning and neoplastic transformation of the mammary gland. The discovery of the metastasis tumor antigen 1 (MTA1) gene, its overexpression in cancer and metastasis and its subsequent identification as an integral part of the chromatin remodeling complex heralded extensive research on its physiological role. Subsequent identification of additional gene family members, namely MTA1s, MTA2, and MTA3, and their functions in the cell has resulted in the establishment of the significance of the MTA family. The role of these proteins in modulating hormonal responses in normal mammary glands and in breast cancer has resulted in their identification as important molecular markers and potential therapeutic targets.

Indexed as

Gene Expression Regulation, NeoplasticMorphogenesisTranscription, GeneticAnimalsBreast NeoplasmsHumansMammary Glands, AnimalMammary Glands, Human

Identifiers

PMID17549610
OpenAlexW2152163156

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.